Cancer Center, Integrated Hospital of Traditional Chinese Medicine, Southern Medical University, Guangzhou, Guangdong, 510315, China.
Cancer center, Southern Medical University, Guangzhou, Guangdong, 510315, China.
J Exp Clin Cancer Res. 2018 Jan 22;37(1):10. doi: 10.1186/s13046-017-0669-z.
The high incidence of recurrence and metastasis of hepatocellular carcinoma (HCC) necessitate the discovery of new predictive biomarkers of invasion and prognosis. Minichromosome maintenance complex component 6 (MCM6), which has been reported to up-regulate in multiple malignancies, was considered to be a novel diagnoses biomarker in HCC. However, its functional contributions and prognostic value remain unclear.
The expression of MCM6 was analyzed in 70 HCC tissues and 5 HCC cell lines by immunohistochemistry and real-time RT-PCR. The roles of MCM6 in HCC cell proliferation, migration and invasion were explored by CCK8, Wound healing and Transwell assays, respectively. Western blotting and Immunofluorescence staining were conducted to detect the protein expressions of ERK signaling pathway and EMT-related markers. To verify the above findings in vivo, we established subcutaneous xenograft tumor and orthotopic xenograft tumor models in nude mice. Finally, Enzyme-linked immunosorbent assay was used to evaluate the serum MCM6 level.
MCM6 was significantly up-regulated in HCC tissues. Increased MCM6 expression was associated with aggressive clinicopathological features and worse prognosis in HCC patients. These results were consistent with our analyses of The Cancer Genome Atlas database (TCGA). Furthermore, knockdown of MCM6 significantly decreased proliferative and migratory/invasive capability of HCC cells in vitro, as well as decreased tumor volume, weight and the number of pulmonary metastases in vivo. Mechanistic analyses indicated that MCM6 promoted EMT and activated MEK/ERK signaling. More importantly, serum MCM6 levels in HCC patients were significantly higher than those in cirrhosis and healthy controls (P < 0.0001), and allowed distinguishing early recurrence with high accuracy (AUC = 0.773).
Our findings indicate that MCM6 predicts poor prognosis and promotes metastasis in HCC. Postoperative serum MCM6 level could be valuable to detect preclinical early recurrence, indicative of a need for more careful surveillance and aggressive therapeutic intervention.
肝细胞癌(HCC)的高复发和转移率需要发现新的侵袭和预后预测生物标志物。微小染色体维持复合物成分 6(MCM6)已在多种恶性肿瘤中上调,被认为是 HCC 的一种新的诊断生物标志物。然而,其功能贡献和预后价值尚不清楚。
通过免疫组化和实时 RT-PCR 分析 70 例 HCC 组织和 5 株 HCC 细胞系中 MCM6 的表达。通过 CCK8、划痕愈合和 Transwell 测定分别探讨 MCM6 在 HCC 细胞增殖、迁移和侵袭中的作用。Western blot 和免疫荧光染色检测 ERK 信号通路和 EMT 相关标志物的蛋白表达。为了在体内验证上述发现,我们在裸鼠中建立了皮下移植瘤和原位移植瘤模型。最后,采用酶联免疫吸附试验检测血清 MCM6 水平。
MCM6 在 HCC 组织中明显上调。MCM6 表达增加与 HCC 患者侵袭性临床病理特征和预后不良相关。这些结果与我们对癌症基因组图谱数据库(TCGA)的分析一致。此外,MCM6 敲低显著降低 HCC 细胞的体外增殖和迁移/侵袭能力,以及体内肿瘤体积、重量和肺转移数。机制分析表明,MCM6 促进 EMT 并激活 MEK/ERK 信号。更重要的是,HCC 患者的血清 MCM6 水平明显高于肝硬化和健康对照组(P<0.0001),并能以高准确度区分早期复发(AUC=0.773)。
我们的研究结果表明,MCM6 预测 HCC 的不良预后和促进转移。术后血清 MCM6 水平可用于检测临床前早期复发,提示需要更仔细的监测和积极的治疗干预。